DBS 3389 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2005-04-22 for DBS 3389 NA manufactured by Medtronic Puerto Rico Operations.

Event Text Entries

[397899] Patient presented with an open right cranial incision in 2005 with light growth of staphylococcus. The device was explanted and returned to the manufacturer for analysis.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number6000153-2005-00636
MDR Report Key594701
Report Source05
Date Received2005-04-22
Date of Report2005-04-04
Date of Event2005-02-23
Date Mfgr Received2005-04-04
Device Manufacturer Date2004-01-01
Date Added to Maude2005-04-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactBARBARA PAHL
Manufacturer Street710 MEDTRONIC PARKWAY
Manufacturer CityMINNEAPOLIS MN 554325604
Manufacturer CountryUS
Manufacturer Postal554325604
Manufacturer Phone7635050856
Manufacturer G1MEDTRONIC PUERTO RICO OPERATIONS
Manufacturer StreetROAD #149, KM. 56.3 CALL BOX 6001
Manufacturer CityVILLALBA PR 00766
Manufacturer CountryUS
Manufacturer Postal Code00766
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDBS
Generic NameLEAD
Product CodeGYZ
Date Received2005-04-22
Returned To Mfg2005-04-04
Model Number3389
Catalog NumberNA
Lot NumberJ0405901V
ID NumberNA
Device Expiration Date2008-01-22
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Age10 MO
Device Eval'ed by MfgrY
Implant FlagY
Date RemovedV
Device Sequence No1
Device Event Key584532
ManufacturerMEDTRONIC PUERTO RICO OPERATIONS
Manufacturer AddressRD. 149, KM. 56.3 CALL BOX 6001 VILLALBA PR 00766 US
Baseline Brand NameDBS
Baseline Generic NameLEAD
Baseline Model No3389
Baseline Catalog NoNA
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-04-22

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